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IFN-gamma-induced BACE1 expression is mediated by activation of JAK2 and ERK1/2 signaling pathways and direct binding of STAT1 to BACE1 promoter in astrocytes.

DC Field Value Language
dc.contributor.authorCho, HJ-
dc.contributor.authorKim, SK-
dc.contributor.authorJin, SM-
dc.contributor.authorHwang, EM-
dc.contributor.authorKim, YS-
dc.contributor.authorHuh, K-
dc.contributor.authorMook-Jung, I-
dc.date.accessioned2011-01-27T04:54:37Z-
dc.date.available2011-01-27T04:54:37Z-
dc.date.issued2007-
dc.identifier.issn0894-1491-
dc.identifier.urihttp://repository.ajou.ac.kr/handle/201003/1335-
dc.description.abstractBeta-site APP cleaving enzyme 1 (BACE1) is an essential enzyme for the production of beta amyloid. Since we found that injection of interferon-gamma (IFN-gamma) into young mouse brains increased BACE1 expression in astrocytes, we investigated molecular mechanisms underlying this process by cloning a putative BACE1 promoter. BACE1 promoter activity was differentially regulated by IFN-gamma in a region specific manner and down-regulated by an inhibitor of Janus kinase 2 (JAK2). A dominant negative mutant of signal transducer and activator of transcription 1 (STAT1) expression suppressed BACE1 promoter activity, and this was rescued by transfecting wild type STAT1. Electrophoretic mobility shift assay and promoter activity assays indicated that STAT1 binds directly to the putative STAT1 binding sequence of BACE1 promoter. Because IFN-gamma treatment induced STAT1 phosphorylation, we examined whether the expression of a suppressor of cytokine signaling (SOCS), negative regulator of JAK2, suppresses BACE1 promoter activity. The results show that SOCS1 or SOCS3 expression suppressed BACE1 promoter by blocking phosphorylation of Tyr701 residue in STAT1. Also, because IFN-gamma treatment specifically potentiated extracellular signal regulated MAP kinase (ERK) 1/2 activation, pretreatment of mitogen-activated or extracellular signal-regulated protein kinase (MEK) inhibitor, PD98059, significantly attenuated IFN-gamma-induced BACE1 promoter activity and protein expression through blocking phosphorylation of Ser727 residue in STAT1, suggesting that ERK1/2 is associated with IFN-gamma-induced STAT1 signaling cascade. Taken together, our results suggest that IFN-gamma activates JAK2 and ERK1/2 and then phosphorylated STAT1 binds to the putative STAT1 binding sequences in BACE1 promoter region to modulate BACE1 protein expression in astrocytes.-
dc.language.isoen-
dc.subject.MESHAlzheimer Disease-
dc.subject.MESHAmyloid Precursor Protein Secretases-
dc.subject.MESHAnimals-
dc.subject.MESHAspartic Acid Endopeptidases-
dc.subject.MESHAstrocytes-
dc.subject.MESHBinding Sites-
dc.subject.MESHBrain-
dc.subject.MESHCell Line, Tumor-
dc.subject.MESHDisease Models, Animal-
dc.subject.MESHEnzyme Activation-
dc.subject.MESHEnzyme Inhibitors-
dc.subject.MESHGene Expression Regulation, Enzymologic-
dc.subject.MESHHumans-
dc.subject.MESHInterferon-gamma-
dc.subject.MESHJanus Kinase 2-
dc.subject.MESHMice-
dc.subject.MESHMitogen-Activated Protein Kinase 3-
dc.subject.MESHPhosphorylation-
dc.subject.MESHPromoter Regions, Genetic-
dc.subject.MESHProtein Binding-
dc.subject.MESHSTAT1 Transcription Factor-
dc.subject.MESHSignal Transduction-
dc.subject.MESHSuppressor of Cytokine Signaling Proteins-
dc.titleIFN-gamma-induced BACE1 expression is mediated by activation of JAK2 and ERK1/2 signaling pathways and direct binding of STAT1 to BACE1 promoter in astrocytes.-
dc.typeArticle-
dc.identifier.pmid17091494-
dc.contributor.affiliatedAuthor허, 균-
dc.type.localJournal Papers-
dc.identifier.doi10.1002/glia.20451-
dc.citation.titleGlia-
dc.citation.volume55-
dc.citation.number3-
dc.citation.date2007-
dc.citation.startPage253-
dc.citation.endPage262-
dc.identifier.bibliographicCitationGlia, 55(3). : 253-262, 2007-
dc.identifier.eissn1098-1136-
dc.relation.journalidJ008941491-
Appears in Collections:
Journal Papers > School of Medicine / Graduate School of Medicine > Medical Humanities & Social Medicine
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